Interesting facts
Interesting Facts about 3’,6’-Dihydroxyspiro[isobenzofuran-3,9’-xanthene]-1-one
3’,6’-Dihydroxyspiro[isobenzofuran-3,9’-xanthene]-1-one is a fascinating compound that has garnered attention due to its unique structure and potential applications in various fields:
- Structural Uniqueness: This compound features a spiro arrangement, which is a characteristic that often contributes to intricate molecular interactions. The spiro structure allows for interesting three-dimensional configurations.
- Photochemical Properties: Compounds like this one are known for their potential in photochemical applications. Their ability to absorb and emit light can enable uses in organic electronics and photosensitizers.
- Biological Relevance: The presence of hydroxyl groups in its structure suggests that it may exhibit biological activity. Compounds with similar configurations have been studied for their anti-cancer and antioxidant properties.
- Dye and Pigment Applications: The structural features of 3’,6’-dihydroxyspiro[isobenzofuran-3,9’-xanthene]-1-one indicate that it may serve as a dye or pigment, particularly in organic colorants. Its vibrant color could be advantageous in various artistic and industrial applications.
- Research Interest: As scientists continue to explore compounds like this, there is a growing interest in synthesizing derivatives to enhance or modify their properties. Such research could lead to the development of new materials with tailored functionalities.
This compound is a prime example of how intricate organic chemistry can lead to materials with diverse potential applications, making it a significant subject for ongoing research.
Synonyms
fluorescein
2321-07-5
Solvent Yellow 94
Resorcinolphthalein
Fluoresceine
Yellow fluorescein
3,6-Fluorandiol
Japan Yellow 201
D and C Yellow No. 7
C.I. Solvent Yellow 94
3',6'-Dihydroxyfluoran
Fluoreszein
Soap Yellow F
Hidacid fluorescein
Fluorescein Red
D+C Yellow No. 7
11712 Yellow
CHEBI:31624
Japan Yellow No. 201
Zlut kysela 73
9-(o-Carboxyphenyl)-6-hydroxy-3-isoxanthenone
9-(o-Carboxyphenyl)-6-hydroxy-3H-xanthen-3-one
Fluoran, 3',6'-dihydroxy-
Dihydroxyfluorane
TPY09G7XIR
Diresorcinolphthalein
C.I. 45350:1
NSC 667256
CCRIS 7076
DTXSID0038887
3',6'-Fluorandiol
HSDB 2128
CI 45350:1
EINECS 219-031-8
UNII-TPY09G7XIR
NSC-667256
NSC-759114
3H-Xanthen-3-one, 9-(o-carboxyphenyl)-6-hydroxy-
BRN 0094324
Ki201
DTXCID8018887
3,6-Dihydroxyspiro(xanthene-9,3'-phthalide)
3',6'-Dihydroxyspiro(isobenzofuran-1(3H),9'(9H)-xanthen)-3-one
D & C YELLOW NO. 7 K7133
3',6'-dihydroxy-3H-spiro[2-benzofuran-1,9'-xanthen]-3-one
FLUORESCEIN (II)
FLUORESCEIN [II]
EC 219-031-8
FLUORESCEIN (MART.)
FLUORESCEIN [MART.]
FLUORESCEIN (USP-RS)
FLUORESCEIN [USP-RS]
5-19-06-00456 (Beilstein Handbook Reference)
Fluorescein (USP:BAN:JAN)
Fluorescein [USP:BAN:JAN]
FLUORESCEIN (EP MONOGRAPH)
FLUORESCEIN [EP MONOGRAPH]
FLUORESCEIN (USP MONOGRAPH)
FLUORESCEIN [USP MONOGRAPH]
3,6-Dihydroxyspiro[xanthene-9,3'-phthalide]
Fluoresceina
3',6'-dihydroxy-3H-spiro(2-benzofuran-1,9'-xanthen)-3-one
fluorescein lactone
D&C yellow No 7
3',4'-Dehydroxyfluoran
3',6'-Dihydroxyfluorane
fluorescein (lactone form)
C.I. 45350 (free acid)
Benzoic acid, 2-(6-Hydroxy-3-oxo-3H-xanthen-9-yl)-,
Benzoic acid, o-(6-hydroxy-3-oxo-3H-xanthen-9-yl)-,
O-(6-HYDROXY-3-OXO-3H-XANTHEN-9-YL)BENZOIC ACID
3',6'-Dihydroxyspiro(isobenzofuran-1(3H), 9'(9H)-xanthen)-3-one
11712 YELLOW9-(O-CARBOXYPHENYL)-6-HYDROXY-3H-XANTHEN-3-ONE
spiro(isobenzofuran-1(3H),9'-(9H)xanthen-3-one, 3',6'-Dihydroxy-
219-031-8
3',6'-Dihydroxy-3H-spiro[isobenzofuran-1,9'-xanthen]-3-one
D&C Yellow No. 7
D & C Yellow no. 7
3',6'-dihydroxyspiro[2-benzofuran-3,9'-xanthene]-1-one
Spiro[isobenzofuran-1(3H),9'-[9H]xanthen]-3-one, 3',6'-dihydroxy-
Fluorescein (free acid)
MFCD00005050
Resorcinol phthalein
CHEMBL1057
NSC667256
Benzoic acid, o-(6-hydroxy-3-oxo-3H-xanthen-9-yl)-
Benzoic acid, 2-(6-hydroxy-3-oxo-3H-xanthen-9-yl)-
NCGC00161643-03
3',6'-Dihydroxyspiro(isobenzofuran-1(3H),9'-(9H)xanthen)-3-one
Spiro(isobenzofuran-1(3H),9'-(9H)xanthen)-3-one, 3',6'-dihydroxy-
CAS-2321-07-5
C20H12O5
Zlut kysela 73 [Czech]
Diofluor
Fluorescite (Salt/Mix)
3',6' dihydroxyfluoran
Fluorescein (JAN/USP)
FLUORESCEIN [MI]
FLUORESCEIN [JAN]
FLUORESCEIN [HSDB]
Epitope ID:137337
UPCMLD-DP087
FLUORESCEIN [VANDF]
SCHEMBL16533
FLUORESCEIN [WHO-DD]
2-(6-Hydroxy-3-oxo-(3H)-xanthen-9-yl)benzoic acid
UPCMLD-DP087:001
GNBHRKFJIUUOQI-UHFFFAOYSA-
Fluorescein (Solvent Yellow 94)
C.I. 45350 (Salt/Mix)
HMS2093F21
HMS3744C17
MOLI001003
Pharmakon1600-01505396
HY-D0251
Tox21_113500
Tox21_303508
BDBM50237588
C.I. Acid Yellow 73 (Salt/Mix)
NSC759114
s5488
Spiro(isobenzofuran-1(3H),9'-(9H)xanthen)-3-one,3'6'-dihydroxy-
AKOS015903296
CCG-213417
CS-7537
DB00693
FF23342
C.I. 45350A
Fluorescein, for fluorescence, free acid
NCGC00161643-01
NCGC00161643-02
NCGC00257491-01
BP-31220
DA-53248
SY012645
SBI-0206827.P001
F0095
Fluorescein (free acid), Dye content 95 %
NS00004148
D01261
D70685
EN300-702817
AB00643381_02
Q410922
SR-05000001696
SR-05000001696-1
BRD-K21913543-001-01-6
BRD-K21913543-001-02-4
3',6'-dihydroxyspiro[isobenzofuran-3,9'-xanthene]-1-one
E89FA0B4-4844-46A2-AF9B-29ECA50E5599
Fluorescein, European Pharmacopoeia (EP) Reference Standard
Fluorescein, United States Pharmacopeia (USP) Reference Standard
3',6'-Dihydroxyspiro[isobenzofuran-1(3H),9'-[9H]xanthen]-3-one;3',6'-Fluorandiol;3,6-Dihydroxyspiro[xanthene-9,3'-phthalide]
InChI=1/C20H12O5/c21-11-5-7-15-17(9-11)24-18-10-12(22)6-8-16(18)20(15)14-4-2-1-3-13(14)19(23)25-20/h1-10,21-22H
Solubility of 3',6'-dihydroxyspiro[isobenzofuran-3,9'-xanthene]-1-one
The solubility characteristics of 3',6'-dihydroxyspiro[isobenzofuran-3,9'-xanthene]-1-one can be assessed based on its structural properties. As a complex organic compound, it exhibits unique interactions with solvents, particularly in terms of polarity.
Solubility Characteristics
In conclusion, while 3',6'-dihydroxyspiro[isobenzofuran-3,9'-xanthene]-1-one shows potential for solubility in polar environments, its practical application may require further empirical studies to determine exact solubility limits in various solvents.